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WO2003010297A1 - Souches de bifidobacterium probiotiques - Google Patents

Souches de bifidobacterium probiotiques Download PDF

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Publication number
WO2003010297A1
WO2003010297A1 PCT/IE2002/000110 IE0200110W WO03010297A1 WO 2003010297 A1 WO2003010297 A1 WO 2003010297A1 IE 0200110 W IE0200110 W IE 0200110W WO 03010297 A1 WO03010297 A1 WO 03010297A1
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WO
WIPO (PCT)
Prior art keywords
formulation
bifidobacterium
strain
disease
bifidobacterium strain
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/IE2002/000110
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English (en)
Inventor
John Kevin Collins
Gerald Christopher O'sullivan
Liam O'mahony
Fergus Shanahan
Barry Kiely
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
PrecisionBiotics Group Ltd
Original Assignee
Alimentary Health Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Alimentary Health Ltd filed Critical Alimentary Health Ltd
Priority to EP02765292A priority Critical patent/EP1409644A1/fr
Priority to AU2002329006A priority patent/AU2002329006A1/en
Priority to CA002454803A priority patent/CA2454803A1/fr
Priority to IL16004802A priority patent/IL160048A0/xx
Priority to BR0211442-9A priority patent/BR0211442A/pt
Priority to JP2003515648A priority patent/JP2005508617A/ja
Priority to MXPA04000738A priority patent/MXPA04000738A/es
Publication of WO2003010297A1 publication Critical patent/WO2003010297A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
    • C12N1/20—Bacteria; Culture media therefor
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/135—Bacteria or derivatives thereof, e.g. probiotics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/66—Microorganisms or materials therefrom
    • A61K35/74—Bacteria
    • A61K35/741—Probiotics
    • A61K35/744—Lactic acid bacteria, e.g. enterococci, pediococci, lactococci, streptococci or leuconostocs
    • A61K35/745—Bifidobacteria
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
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    • A—HUMAN NECESSITIES
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    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • A—HUMAN NECESSITIES
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/06—Antianaemics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
    • C12N1/20—Bacteria; Culture media therefor
    • C12N1/205—Bacterial isolates
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2400/00—Lactic or propionic acid bacteria
    • A23V2400/51—Bifidobacterium
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2400/00—Lactic or propionic acid bacteria
    • A23V2400/51—Bifidobacterium
    • A23V2400/533—Longum
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
    • C12R2001/00—Microorganisms ; Processes using microorganisms
    • C12R2001/01—Bacteria or Actinomycetales ; using bacteria or Actinomycetales
    • C12R2001/02—Acetobacter

Definitions

  • the defense mechanisms to protect the human gastrointestinal tract from colonization by intestinal bacteria are highly complex and involve both immunological and non- immunological aspects (1).
  • Innate defense mechanisms include the low pH of the stomach, bile salts, peristalsis, mucin layers and anti-microbial compounds such as lysozyme (2).
  • Immunological mechanisms include specialized lymphoid aggregates, underlying M cells, called peyers patches which are distributed throughout the small intestine and colon (3). Luminal antigens presented at these sites result in stimulation of appropriate T and B cell subsets with establishment of cytokine networks and secretion of antibodies into the gastrointestinal tract (4).
  • antigen presentation may occur via epithelial cells to intraepithelial lymphocytes and to the underlying lamina limba immune cells (5). Therefore, the host invests substantially in immunological defense of the gastrointestinal tract.
  • the gastrointestinal mucosa is the largest surface at which the host interacts with the external environment, specific control mechanisms must be in place to regulate immune responsiveness to the 100 tons of food which is handled by the gastrointestinal tract over an average lifetime.
  • the gut is colonized by over 500 species of bacteria numbering 10 ⁇ -10 12 /g in the colon.
  • these control mechanisms must be capable of distinguishing non-pathogenic adherent bacteria from invasive pathogens, which would cause significant damage to the host.
  • the intestinal flora contributes to defense of the host by competing with newly ingested potentially pathogenic micro-organisms.
  • the formulation includes a prebiotic material.
  • the invention is therefore of major potential therapeutic value in the prophylaxis or treatment of dysregulated immune responses, such as undesirable inflammatory reactions for example inflammatory bowel disease.
  • a deposit of Bifidobacterium longum infantis strain AH212 was made at the NCIMB on March 22, 2001 and accorded the accession number NCIMB 41099.
  • Fig. 1 is a bar graph showing the adhesive nature of Bifidobacterium longum infantis to human gastrointestinal epithelial cells, CaCo-2 and HT-29;
  • Fig. 2 is a bar graph showing the effect of each Bifidobacterium longum infantis strain on IFN ⁇ (pg/ml) production by PBMCs;
  • Fig. 4 is a bar graph showing the IL-12 (pg/ml) response of PBMCs following co-incubation with Bifidobacterium longum infantis;
  • Fig. 5 is a bar graph illustrating the non-stimulatory effect of Bifidobacterium longum infantis on LL-8 production.
  • IL-12 is a heterodimeric protein of 70 kD composed of two covalently linked chains of
  • TNF ⁇ is a proinflammatory cytokine which mediates many of the local and systemic effects seen during an inflammatory response.
  • This cytokine is primarily a monocyte or macrophage derived product but other cell types including lymphocytes, neutrophils, NK cells, mast cells, astrocytes, epithelial cells endothelial cells and smooth muscle cells can also synthesise TNF ⁇ .
  • TNF ⁇ is synthesised as a prohormone and following processing the mature 17.5 kDa species can be observed. Purified
  • Example 1 Characterisation of bacteria isolated from resected and washed human gastrointestinal tract. Demonstration of probiotic traits.
  • Frozen tissues were thawed, weighed and placed in cysteinated (0.05%) one quarter strength Ringers ' solution. The sample was gently shaken to remove loosely adhering microorganisms (termed -wash 'W'). Following transfer to a second volume of Ringer's solution, the sample was vortexed for 7 mins to remove tightly adhering bacteria (termed -sample 'S'). In order to isolate tissue embedded bacteria, samples 356, 176 and A were also homogenized in a Braun blender (termed -homogenate ⁇ ').
  • the solutions were serially diluted and spread-plated (lOO ⁇ l) on the following agar media: RCM (reinforced clostridia media) and RCM adjusted to pH 5.5 using acetic acid; TPY (trypticase, peptone and yeast extract); MRS (deMann, Rogosa and Sharpe); ROG (acetate medium (SL) of Rogosa); LLA (liver-lactose agar of Lapiere); BHI (brain heart infusion agar); LBS (Bifidobacterium selective agar) and TSAYE (tryptone soya sugar supplemented with 0.6% yeast extract).
  • RCM reinforcementd clostridia media
  • TPY trypticase, peptone and yeast extract
  • MRS deMann, Rogosa and Sharpe
  • ROG acetate medium (SL) of Rogosa)
  • LLA liver-lactose agar of Lapiere
  • BHI brain
  • Table 1 shows the bacterial counts of tissue samples expressed as colony forming units per gram (cfu/ml) of tissue.
  • TPYP 0 >9.0 x 10 3 >6.0 x 10 3 >3.0 x 10 4 0 1.9 x lO 2 2.8 x 10 2
  • ROG 0 >9.0 x 10 3 >6.0 x 10 3 7.7 x 10 2 3.8 x lO 2 9.7 x 10 1 4.0 x 10 1
  • BIFID- acetate actate, 3:2; ND, Not Determined; REDn, Reduction; Rp, Partial reduction, Cc, Complete reduction;
  • Bifidobacterium isolates were grown up on TPY agar as described above. Cells were resuspended in the medium provided, inoculated into the strips and after 4h the strips were read according to the manufacturer's instructions.
  • Human gastric juice was obtained from healthy subjects by aspiration through a nasogastric tube (Mercy Hospital, Cork, Ireland). It was immediately centrifuged at 13,000 g for 30 min to remove all solid particles, sterilised through 0.45 ⁇ m and 0.2 ⁇ m filters and divided into 40 ml aliquots which were stored at 4°C and -20°C.
  • the indicator microorganisms used in this study many of which are wild type strains isolated in Wind Hospital, Cork, Ireland, were propagated in the following medium under the following growth conditions: Staphylococcus (37°C, anaerobic), Bacillus
  • Indicators used in the initial screening were L. innocua, L. fermentum KLD, P. flourescens and E. coli V157. Briefly, the bifidobacteria (TPY) were incubated for 36-48 h. Ten-fold serial dilutions were spread-plated (lOO ⁇ l) onto TPY agar medium. After overnight incubation, plates with distinct colonies were overlayed with the indicator bacterium. The indicator lawn was prepared by inoculating a molten overlay with 2% (v/v) of an overnight indicator culture which was poured over the surface of the inoculated TPY plates.
  • Table 8 below shows the inhibition of Pseudomonas and Bacillus strains.
  • Example 2 Adhesion of probiotic bacteria to gastrointestinal epithelial cells.
  • the adhesion of the probiotic strains was carried out using a modified version of a previously described method (23).
  • the monolayers of HT-29 and Caco-2 cells were prepared on sterile 22mm 2 glass coverslips, which were placed in Corning tissue culture dishes, at a concentration of 4 X 10 4 cells/ml. Cells were fed fresh medium every 2 days. After ⁇ 10 days, and differentiation of the monolayer had occurred, the monolayers were washed twice with Phosphate Buffered Saline (PBS).
  • PBS Phosphate Buffered Saline
  • TNF ⁇ extracellular cytokine levels were measured using standard ELISA kits (R&D Systems). TNF ⁇ levels levels were measured, in duplicate, using PBMCs from 3 healthy volunteers.
  • the human immune system plays a significant role in the aetiology and pathology of a vast range of human diseases. Hyper and hypo-immune responsiveness results in, or is a component of, the majority of disease states.
  • One family of biological entities, termed cytokines, are particularly important to the control of immune processes. Pertubances of these delicate cytokine networks are being increasingly associated with many diseases.
  • the enteric flora is important to the development and proper function of the intestinal immune system. In the absence of an enteric flora, the intestinal immune system is underdeveloped, as demonstrated in germ free animal models, and certain functional parameters are diminished, such as macrophage phagocytic ability and immunoglobulin production (24). The importance of the gut flora in stimulating non- damaging immune responses is becoming more evident. The increase in incidence and severity of allergies in the western world has been linked with an increase in hygiene and sanitation, concomitant with a decrease in the number and range of infectious challenges encountered by the host. This lack of immune stimulation may allow the host to react to non-pathogenic, but antigenic, agents resulting in allergy or autoimmunity. Deliberate consumption of a series of non-pathogenic immunomodulatory bacteria would provide the host with the necessary and appropriate educational stimuli for proper development and control of immune function. Inflammation
  • Cytokine cascades and networks control the inflammatory response rather than the action of a particular cytokine on a particular cell type (26). Waning of the inflammatory response results in lower concentrations of the appropriate activating signals and other inflammatory mediators leading to the cessation of the inflammatory response.
  • TNF ⁇ is a pivotal proinflammatory cytokine as it initiates a cascade of cytokines and biological effects resulting in the inflammatory state. Therefore, agents which inhibit TNF ⁇ are currently being used for the treatment of inflammatory diseases, e.g. infliximab.
  • strains of the present invention may have potential application in the treatment of a range of inflammatory diseases, particularly if used in combination with other anti- inflammatory therapies, such as non-steroid anti-inflammatory drugs (NSAIDs) or Infliximab.
  • NSAIDs non-steroid anti-inflammatory drugs
  • Infliximab Infliximab
  • the inflammatory response may have significant roles to play in the above mechanisms, thus contributing to the decline of the host and progression of the tumour.
  • intestinal bacteria can produce, from dietary compounds, substances with genotoxic, carcinogenic and tumour-promoting activity and gut bacteria can activate pro- carcinogens to DNA reactive agents (29).
  • species of Bifidobacterium have low activities of xenobiotic metabolizing enzymes compared to other populations within the gut such as bacteroides, eubacteria and clostridia. Therefore, increasing the number of Bifidobacterium bacteria in the gut could beneficially modify the levels of these enzymes.
  • TTFC tetanus toxin fragment C
  • probiotic organisms The introduction of probiotic organisms is accomplished by the ingestion of the microorganism in a suitable carrier. It would be advantageous to provide a medium that would promote the growth of these probiotic strains in the large bowel.
  • the addition of one or more oligosaccharides, polysaccharides, or other prebiotics enhances the growth of lactic acid bacteria in the gastrointestinal tract.
  • Prebiotics refers to any non- viable food component that is specifically fermented in the colon by indigenous bacteria thought to be of positive value, e.g. bifidobacteria, lactobacilli. Types of prebiotics may include those that contain fructose, xylose, soya, galactose, glucose and mannose.
  • the combined administration of a probiotic strain with one or more prebiotic compounds may enhance the growth of the administered probiotic in vivo resulting in a more pronounced health benefit, and is termed synbiotic.
  • Other active ingredients may enhance the growth of the administered probiotic in vivo
  • the probiotic strains may be administered prophylactically or as a method of treatment either on its own or with other probiotic and/or prebiotic materials as described above.
  • the bacteria may be used as part of a prophylactic or treatment regime using other active materials such as those used for treating inflammation or other disorders especially those with an immunological involvement.
  • Such combinations may be administered in a single formulation or as separate formulations administered at the same or different times and using the same or different routes of administration.
  • IL-10 strongly reduce antigen-specific human T cell proliferation by diminishing the antigen-presenting capacity of monocytes via downregulation of class II major histocompatibility complex expression. J Exp Med 1991 Oct l;174(4):915-24.

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Abstract

Cette invention concerne une souche de Bifidobacterium, AH208, AH209, AH210, AH211, AH212 ou AH214, ou des mutants ou des variantes de cette souche, pouvant être utilisés dans la prophylaxie et/ou le traitement d'une activité inflammatoire, en particulier une activité inflammatoire gastro-intestinale indésirable, telle que la maladie entérique inflammatoire ou le syndrome du côlon irritable.
PCT/IE2002/000110 2001-07-26 2002-07-26 Souches de bifidobacterium probiotiques Ceased WO2003010297A1 (fr)

Priority Applications (7)

Application Number Priority Date Filing Date Title
EP02765292A EP1409644A1 (fr) 2001-07-26 2002-07-26 Souches de bifidobacterium probiotiques
AU2002329006A AU2002329006A1 (en) 2001-07-26 2002-07-26 Probiotic bifidobacterium strains
CA002454803A CA2454803A1 (fr) 2001-07-26 2002-07-26 Souches de bifidobacterium probiotiques
IL16004802A IL160048A0 (en) 2001-07-26 2002-07-26 Probiotic bifidobacterium strains
BR0211442-9A BR0211442A (pt) 2001-07-26 2002-07-26 Cepas de bifidobacterium probióticas
JP2003515648A JP2005508617A (ja) 2001-07-26 2002-07-26 プロバイオティックビフィドバクテリウム株類
MXPA04000738A MXPA04000738A (es) 2001-07-26 2002-07-26 Cepas de bifidobacterium probiotico.

Applications Claiming Priority (12)

Application Number Priority Date Filing Date Title
IE010709 2001-07-26
IE20010711 2001-07-26
IE010713 2001-07-26
IE010717 2001-07-26
IE010714 2001-07-26
IE20010710 2001-07-26
IE010710 2001-07-26
IE20010709 2001-07-26
IE010711 2001-07-26
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